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Regulatory Affairs Strategist

hace 2 meses

Xico, México Thermo Fisher Scientific A tiempo completo
Job Summary

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Thermo Fisher Scientific. As a key member of our Regulatory Liaison team, you will play a critical role in leading communications with regulatory agencies and providing regulatory affairs strategy and technical/project leadership on a regional/global level.

Key Responsibilities:
  • Provide regulatory advice and carry out projects in the provision of regulatory affairs services.
  • Act as liaison with internal stakeholders in the provision of these services.
  • Work with the Regulatory Affairs Management to perform the day-to-day operational aspects of the Department such as assessment of regulatory documents, preparation and assembly of global regulatory submissions, QC review of the final submission package.
  • Interface with PPD project teams and Health Authorities regarding regulatory strategy/submission activities.
  • Develop and maintain a cooperative working relationship with Project Managers and project team members for assigned projects.
  • Advises and directs project team as to their responsibilities relative to regulatory strategy/submission activities.
  • Act as a key liaison between Regulatory Affairs Department and project team for assigned projects.
Requirements:
  • Bachelor's Degree; degree in Pharmacy or Life Science is an advantage.
  • Previous regulatory experience, or a combination of higher education/less experience, or substitution of equivalent relevant work experience will be considered.
  • Some regulatory affairs experience is preferable but not mandatory.
  • An appreciation of the requirements, timelines, and processes for regulatory applications globally is a valuable asset.
  • Previous experience with clinical trials application compilation and submissions in the EU and other countries is an advantage.
  • Excellent English language communication skills, both verbal and in writing.
  • Computer skills (Microsoft Office) and experience in applications used in clinical trials (eTMF, CTMS) would be an advantage.
  • Good organizational and planning skills; ability for multiple project tasking.
  • Proven ability to work effectively in a team, including in a multinational one.
  • Problem-solving skills and strong attention to detail.